GENOMEPEP · UNCOVERING PATHOGENIC MICROPEPTIDES FROM THE HUMAN GENOME
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2020-09-01 → 2024-01-01
- EU contribution
- €213,290
- Participants
- 1
- Scheme
- MSCA-IF
Lines connect the coordinator with its partners.
Results in brief
UNCOVERING PATHOGENIC MICROPEPTIDES FROM THE HUMAN GENOME
In recent years, a striking number of regions of the genome have been discovered to be capable of being transcribed and translated into short polypeptides. These micropeptides comprise of fewer than 100 amino acids and thousands of new micropeptide encoding genes have been proposed to exist within the human genome. These novel genes are hypothesized to participate in numerous molecular, cellular, and physiological processes, yet the function of but a few of them has been identified. The GENOMEPEP project concentrated on developing analysis pipelines to carry out analyses concentrating on identifying potentially pathogenic micropeptides. This project leveraged existing data from the Estonian Biobank, which includes genotyping of 212,000 volunteers using DNA microarrays and imputed data for common and rare variants. With access to comprehensive digital health records since 2004, the project utilized diagnostic codes and phenotypes to create detailed study cohorts, facilitated by the digitalized Estonian healthcare system. The project's first phase involved compiling these diverse datasets to establish cohorts focused on cardiovascular and related diseases, utilizing additional data such as blood metabolite information and prescription medicine data for cohort stratification. The second phase concentrates on identifying pathogenic variants within the micropeptidome that correlate with cardiovascular phenotypes and other traits through GWAS and subsequent analyses, with contingencies for non-significant findings. Identification of novel pathogenic genes and development of guidelines to investigate the micropeptidome will assist in the advancement of research, diagnostic medicine, and pharmacology both in the public and private sectors.
Data: CORDIS, © European Union
Project objective
The human genome is over 3 billion nucleotides long, yet only 1,5% of it codes for proteins. In recent years, a striking number of regions of the genome have been discovered to be capable of being transcribed and translated into short polypeptides. These micropeptides comprise of less than 100 amino acids and to date, more than 160 000 different micropeptides have been catalogued within human tissues. These protein products are hypothesized to participate in numerous molecular, cellular and physiological processes, yet the function of but a few micropeptides has been identified. Subsequently, due to its largely unknown functionality, the micropeptidome is commonly overlooked during genomic studies.Due to increasing life expectancy and detrimental lifestyle habits, the European population can be considered to be a high-risk population for cardiovascular diseases, which cause millions of deaths per annum, while taking a tremendous financial toll on the regional economy. GENOMEPEP aims to pinpoint novel micropeptides participating in the pathogenesis of cardiovascular diseases by investigating the genetic variation within the micropeptidome-encoding genome in correlation to existing common cardiovascular phenotypes in population. This will be achieved by establishing a computational analysis pipeline based on biometric, genotype and health records data available within the Estonian and Finnish biobanks. The identification of novel pathogenic genes and the development of guidelines to investigate the micropeptidome would assist in the advancement of research, diagnostic medicine and pharmacology both in public and private sectors.The results of GENOMEPEP will address the CVD research aspect highlighted in “Societal Challenge 1” work program of Horizon 2020, as well as improve other research priorities set by Horizon 2020, e.g. the progression of personalized medicine and support the decrease of economic burden by healthcare.
Original text from CORDIS.
Participants
- TARTU ULIKOOL · TartuCoordinatorEstonia
Links
- View on CORDIS
- DOI: 10.3030/894987
- https://www.etis.ee/Portal/Projects/Display/c1fedb68-b65e-463f-9e21-b2caf1a035e8
Data: CORDIS, © European Union
